[(R)-2-(tert-Butyl-diphenyl-silanyloxy)-3-(tetrahydro-pyran-2-yloxy)-propylsulfanyl]-acetic acid ethyl ester

Base Information

• Chemical Name: [(R)-2-(tert-Butyl-diphenyl-silanyloxy)-3-(tetrahydro-pyran-2-yloxy)-propylsulfanyl]-acetic acid ethyl ester
• CAS No.: 106867-42-9
• Molecular Formula: C₂₈H₄₀O₅SSi
• Molecular Weight: 516.774
• Mol file: 106867-42-9.mol

Synonyms:[(R)-2-(tert-Butyl-diphenyl-silanyloxy)-3-(tetrahydro-pyran-2-yloxy)-propylsulfanyl]-acetic acid ethyl ester

Chemical Property of [(R)-2-(tert-Butyl-diphenyl-silanyloxy)-3-(tetrahydro-pyran-2-yloxy)-propylsulfanyl]-acetic acid ethyl ester

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of [(R)-2-(tert-Butyl-diphenyl-silanyloxy)-3-(tetrahydro-pyran-2-yloxy)-propylsulfanyl]-acetic acid ethyl ester

There total 2 articles about [(R)-2-(tert-Butyl-diphenyl-silanyloxy)-3-(tetrahydro-pyran-2-yloxy)-propylsulfanyl]-acetic acid ethyl ester which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 98.0%

[(R)-2-Hydroxy-3-(tetrahydro-pyran-2-yloxy)-propylsulfanyl]-acetic acid ethyl ester (106851-44-9) + tert-butylchlorodiphenylsilane (58479-61-1) → [(R)-2-(tert-Butyl-diphenyl-silanyloxy)-3-(tetrahydro-pyran-2-yloxy)-propylsulfanyl]-acetic acid ethyl ester (106867-42-9)

Guidance literature:

With 1H-imidazole; In N,N-dimethyl-formamide; at 50 ℃; for 24h;

DOI:10.1016/S0040-4039(00)84291-4

Reference yield:

2-((R)-oxiran-2-ylmethoxy)tetrahydro-2H-pyran (110657-96-0) → [(R)-2-(tert-Butyl-diphenyl-silanyloxy)-3-(tetrahydro-pyran-2-yloxy)-propylsulfanyl]-acetic acid ethyl ester (106867-42-9)

Guidance literature:

Multi-step reaction with 2 steps

1: 99 percent / NaOEt / ethanol / 22 °C

2: 98 percent / imidazole / dimethylformamide / 24 h / 50 °C

With 1H-imidazole; sodium ethanolate; In ethanol; N,N-dimethyl-formamide;

DOI:10.1016/S0040-4039(00)84291-4

Reference yield: 96.0%

[(R)-2-(tert-Butyl-diphenyl-silanyloxy)-3-(tetrahydro-pyran-2-yloxy)-propylsulfanyl]-acetic acid ethyl ester (106867-42-9) → 2-[(R)-2-(tert-Butyl-diphenyl-silanyloxy)-3-(tetrahydro-pyran-2-yloxy)-propylsulfanyl]-ethanol (106851-39-2)

Guidance literature:

With lithium aluminium tetrahydride; In tetrahydrofuran; at 0 ℃; for 3h;

DOI:10.1016/S0040-4039(00)84291-4

upstream raw materials:

[(R)-2-Hydroxy-3-(tetrahydro-pyran-2-yloxy)-propylsulfanyl]-acetic acid ethyl ester

tert-butylchlorodiphenylsilane

2-((R)-oxiran-2-ylmethoxy)tetrahydro-2H-pyran

Downstream raw materials:

2-[(R)-2-(tert-Butyl-diphenyl-silanyloxy)-3-(tetrahydro-pyran-2-yloxy)-propylsulfanyl]-ethanol

(R)-2-(tert-Butyl-diphenyl-silanyloxy)-3-vinylsulfanyl-propionaldehyde

(2E,4E)-(R)-6-(tert-Butyl-diphenyl-silanyloxy)-7-vinylsulfanyl-hepta-2,4-dienoic acid methyl ester

tert-Butyl-[(R)-1-(2-chloro-ethylsulfanylmethyl)-2-(tetrahydro-pyran-2-yloxy)-ethoxy]-diphenyl-silane